| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g39900 | A02 | 33765888 | C | T | missense_variant | MODERATE | c.1477G>A|p.Asp493Asn |
S98 |
| 2 | BAA02g39900 | A02 | 33766587 | C | T | missense_variant | MODERATE | c.778G>A|p.Glu260Lys |
S260 |
| 3 | BAA02g39900 | A02 | 33767699 | G | A | synonymous_variant | LOW | c.339C>T|p.Ile113Ile |
S221 |
| 4 | BAA02g39900 | A02 | 33772124 | C | T | upstream_gene_variant | MODIFIER | c.-3900G>A| |
S271 |
| 5 | BAA02g39900 | A02 | 33772333 | G | A | upstream_gene_variant | MODIFIER | c.-4109C>T| |
S110 |
| 6 | BAA02g39900 | A02 | 33772384 | A | T | upstream_gene_variant | MODIFIER | c.-4160T>A| |
S217 S248 |
| 7 | BAA02g39900 | A02 | 33772625 | T | A | upstream_gene_variant | MODIFIER | c.-4401A>T| |
S33 |
| 8 | BAA02g39900 | A02 | 33773064 | G | A | upstream_gene_variant | MODIFIER | c.-4840C>T| |
S36 |
| 9 | BAA02g39900 | A02 | 33773098 | G | A | upstream_gene_variant | MODIFIER | c.-4874C>T| |
S306 S308 |